Canonical Allele Identifier: CA368991791

Gene: MET

Linked Data

• dbSNP Id: rs121913677
• MyVariant Identifiers: chr7:g.116423456A>T (hg19) ; chr7:g.116783402A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116783402A>T , CM000669.2:g.116783402A>T	GRCh38
NC_000007.13:g.116423456A>T , CM000669.1:g.116423456A>T	GRCh37
NC_000007.12:g.116210692A>T	NCBI36
NG_008996.1:g.115998A>T , LRG_662:g.115998A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000436117.3:c.*1336A>T	ENSP00000410980.2:n.*1336A>T
ENST00000318493.11:c.3785A>T	ENSP00000317272.6:p.Lys1262Met
ENST00000397752.8:c.3731A>T MANE Select	ENSP00000380860.3:p.Lys1244Met
ENST00000318493.10:c.3785A>T	ENSP00000317272.6:p.Lys1262Met
ENST00000397752.7:c.3731A>T	ENSP00000380860.3:p.Lys1244Met
NM_000245.2:c.3731A>T	NP_000236.2:p.Lys1244Met
NM_001127500.1:c.3785A>T , LRG_662t1:c.3785A>T	NP_001120972.1:p.Lys1262Met
XM_006715990.2:c.2441A>T	XP_006716053.1:p.Lys814Met
XM_006715991.2:c.2441A>T	XP_006716054.1:p.Lys814Met
XM_011516223.1:c.3788A>T	XP_011514525.1:p.Lys1263Met
NM_000245.3:c.3731A>T	NP_000236.2:p.Lys1244Met
NM_001127500.2:c.3785A>T	NP_001120972.1:p.Lys1262Met
NM_001324402.1:c.2441A>T	NP_001311331.1:p.Lys814Met
XR_001744772.1:n.3862A>T
NM_001127500.3:c.3785A>T	NP_001120972.1:p.Lys1262Met
NM_000245.4:c.3731A>T MANE Select	NP_000236.2:p.Lys1244Met
NM_001324402.2:c.2441A>T	NP_001311331.1:p.Lys814Met